Power Knee

Power Knee Batt Charger Loaner

Registry build 21.09.26
1manufacturer
11catalogue numbers in this listing
1recall

Who Else Makes It

Registered in Jiangsu.

Chinese manufacturers registered for FDA product code ISW
Manufacturer City Province Registered as Device types
Yangzhou Sensport Healthcare Supplies Co., Ltd. Yangzhou Jiangsu Manufacturer 27

Record

Regulatory record for Power Knee
Listed by Ossur Americas, United States
FDA product code ISW
Device type Assembly, Knee/Shank/Ankle/Foot, External
Device class Class 2
Regulation 21 CFR 890.3500
Establishment Contract manufacturer, Repacker / relabeller, Manufacturer
Premarket notification Exempt
Record published 2018-05-16
Record revised 2025-07-01 (version 2)

Specifications

Specifications
MRI safety Labeling does not contain MRI Safety Information
Prescription Prescription only
Label carries manufacturing date, serial number
Storage Handling environment temperature -10 to 40 °C; Handling environment humidity 0 to 100 % RH; Storage environment humidity 0 to 90 % RH; Storage environment temperature 0 to 45 °C
Distribution end date 2021-12-17

Catalogue Numbers

Catalogue numbers for Power Knee
Catalogue number Size Status
PKN12100 Withdrawn
PK22100 Withdrawn
PKN123007 Withdrawn
PKN120007 Withdrawn
PK230010 Withdrawn
PKN120037 Withdrawn
PK220007 Withdrawn
PKN120017 Withdrawn
PK23100 Withdrawn
PK218001 Withdrawn
PK218000 Withdrawn

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Empower Otto Bock Healthcare GmbH 621
Symbionic Leg Ossur Americas 118
Walkasins Rxfunction Inc. 18
BiOM T2 Bionx Medical Technologies, Inc. 9
emPOWER Bionx Medical Technologies, Inc. 7
Bio Leg™ Bionicm 4
Rheo Knee Ossur Americas 3
BiOM T2 Otto Bock Healthcare GmbH 2
C-Matt Casco Manufacturing Solutions, Inc. 1

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity
2022-08-29 Class II Device Design Battery may dislodge from the Power Knee 190 devices

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer